Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2071375
rs2071375
1 1.000 0.080 2 112777861 intron variant C/T snv 0.26 0.010 1.000 1 2012 2012